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Interface engineered multifunctional oxide thin films with optimized properties.

机译:具有优化性能的界面工程多功能氧化物薄膜。

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摘要

In our world today, energy has become one of the most valuable resources, in particular, renewable and clean energy sources. The research presented here represents an investigation into three separate areas of this topic. In thin film applications, the ordered structures as well as the inherent thinness of the films precludes the normal physics found in bulk materials. Characterizations of films of this type can provide information on molecular level charge transfer processes of the film layer materials since diffusive properties are minimal. With the control given by pulsed laser deposition methods, film and interface structure can be altered allowing for an examination of these effects on the materials properties. For the electrolyte and cathode materials, this equates to finding thermal and PO2 dependencies for electronic and ionic transport. For barium titanate, aside from the effects of oxygen vacancies, the interface quality between the electrodes and the ferroelectric material determines the effectiveness of energy transfer between these boundaries. That is, poor bonding characteristics or the formation of intermediate layers will introduce inconsistencies and (possibly) unwanted piezoelectric response properties of the material which could introduce parasitic dampening (resistance) of the mechanical vibrations of a piezoelectric transducer, altering its resonant characteristics.;The clean reaction products and potential for high power outputs provide a strong impetus into investigations of fuel cell structures to improve their functionality. With conventional applications being dominated by high temperature (>700 °C) cells utilizing YSZ as an electrolyte medium, much gain can be made in efficiency through the lowering of cell operation temperature. The first part of my research focuses on the growth and characterization of a novel multilayered electrolyte structure consisting of alternating layers of GCO and YSZ for use in a medium temperature (400--600 °C) application. Half-cell and whole-cell structures were grown using PLD methods and were characterized using XRD, SEM, TEM and EIS. This multilayered electrolyte structure was found to have a lower activation energy than that previously reported for bulk materials and was found to produce peak power at approximately 600 °C.;The second part of this research focused on the growth and characterization of half-cell structures utilizing the perovskite LBCO as the cathode surface and GCO as the electrolyte material. Characterization was performed with XRD, EIS and TEM. Temperature dependent EIS results indicate that found that the oxygen uptake at the interface is fast with an activation energy of approximately 0.46 eV. It was found that the surface oxygen adsorption process is complicated and possibly the product of several rate limiting processes including possibly dissociative adsorption. It was also found that when combined with gadolinia doped ceria as an electrolyte that the interface grain boundaries are influenced by the deposition oxygen partial pressures. The rapid oxygen uptake and low activation energy makes this material a possible candidate for further testing in SOFC applications.;The final part of the presented research focused on non-standard deposition conditions of BTO on various substrate materials, including flexible carbon fiber fabric, using PLD methods along with a characterization of these films to explore its application in energy harvesting applications. Perovskites are part of the Ruddlesden-Popper family, with the crystal structure A n+1Bn O3n+1, with n = infinity. Barium titanate (BTO) is a member of the perovskite family and has gained notice not only for its excellent dielectric properties but also as a promising, non-lead-containing, ferroelectric material. Dependency on oxygen partial pressure during film growth was found to have a profound effect on the remnant polarization response and ferroelectric response was observed in films grown at temperatures down to 200 °C. Piezoelectric measurements were made with a resulting measured electric field of 0.4kV/m and a calculated d31 component of 2.74 X 10-14 pC/N. The reasons for this very low (2 orders of magnitude lower than in literature) d31 component are found, by considering the relevant contributions, to be related to the properties of the chosen carbon fiber fabric. However, it was shown that low temperature deposition of barium titanate produced films with reasonable ferroelectric and piezoelectric properties allowing for possible use in some energy harvesting applications.
机译:在当今世界,能源已成为最有价值的资源之一,尤其是可再生和清洁能源。本文介绍的研究代表了对该主题三个独立领域的调查。在薄膜应用中,薄膜的有序结构以及固有的薄度妨碍了散装材料中常见的物理性质。这种类型的薄膜的特征可以提供关于薄膜层材料的分子级电荷转移过程的信息,因为扩散特性极小。通过脉冲激光沉积方法的控制,可以改变薄膜和界面结构,从而可以检查这些对材料性能的影响。对于电解质和阴极材料,这相当于找到电子和离子传输的热和PO2依赖性。对于钛酸钡,除了氧空位的影响外,电极与铁电材料之间的界面质量还决定了这些边界之间能量转移的有效性。也就是说,不良的粘合特性或中间层的形成将导致材料的不一致性和(可能)有害的压电响应特性,这可能会引入压电换能器的机械振动的寄生阻尼(电阻),从而改变其谐振特性。清洁的反应产物和高功率输出的潜力为研究燃料电池结构以改善其功能提供了强大的动力。在常规应用中,以YSZ作为电解质介质的高温(> 700°C)电池占主导地位,通过降低电池工作温度,可以在效率上获得很大的收益。我的研究的第一部分专注于新型多层电解质结构的生长和表征,该结构由GCO和YSZ的交替层组成,适用于中等温度(400--600°C)应用。半细胞和全细胞结构使用PLD方法生长,并使用XRD,SEM,TEM和EIS进行表征。发现这种多层电解质结构的活化能比以前报道的散装材料低,并在约600°C时产生峰值功率;该研究的第二部分着重于半电池结构的生长和表征利用钙钛矿LBCO作为阴极表面,GCO作为电解质材料。用XRD,EIS和TEM进行表征。温度相关的EIS结果表明,发现界面处的氧气吸收很快,活化能约为0.46 eV。已经发现,表面氧吸附过程是复杂的,并且可能是几种速率限制过程的产物,包括可能的离解吸附。还发现当与掺杂氧化ado的二氧化铈作为电解质组合时,界面晶粒边界受沉积氧分压的影响。快速的氧气吸收和低的活化能使该材料成为SOFC应用中进一步测试的可能候选材料。 PLD方法以及这些薄膜的特性,以探索其在能量收集应用中的应用。钙钛矿是Ruddlesden-Popper家族的一部分,晶体结构为A n + 1Bn O3n + 1,n =无穷大。钛酸钡(BTO)是钙钛矿家族的成员,不仅因其出色的介电性能而获得关注,而且作为一种有前途的,不含铅的铁电材料而受到关注。发现在膜生长期间对氧分压的依赖性对残余极化响应具有深远的影响,并且在低至200°C的温度下生长的膜中观察到铁电响应。进行压电测量,得到的测量电场为0.4kV / m,计算出的d31分量为2.74 X 10-14 pC / N。通过考虑相关贡献,发现了这种极低(比文献中低2个数量级)的d31组分的原因,与所选碳纤维织物的性能有关。然而,已经表明,钛酸钡的低温沉积产生具有合理的铁电和压电性质的膜,从而允许在某些能量收集应用中使用。

著录项

  • 作者

    Collins, Gregory Roy.;

  • 作者单位

    The University of Texas at San Antonio.;

  • 授予单位 The University of Texas at San Antonio.;
  • 学科 Physics Condensed Matter.;Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 133 p.
  • 总页数 133
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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